Canonical Allele Identifier: CA377670490

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1406158087
• gnomAD v2: 10-96540294-C-G
• gnomAD v4: 10-94780537-C-G
• MyVariant Identifiers: chr10:g.96540294C>G (hg19) ; chr10:g.94780537C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780537C>G , CM000672.2:g.94780537C>G	GRCh38
NC_000010.10:g.96540294C>G , CM000672.1:g.96540294C>G	GRCh37
NC_000010.9:g.96530284C>G	NCBI36
NG_008384.2:g.22832C>G
NG_008384.3:g.22857C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.520C>G MANE Select	ENSP00000360372.3:p.Pro174Ala
ENST00000645461.1:n.1573C>G
ENST00000371321.7:c.520C>G	ENSP00000360372.3:p.Pro174Ala
ENST00000464755.1:c.1283C>G	ENSP00000483243.1:n.1283C>G
NM_000769.2:c.520C>G	NP_000760.1:p.Pro174Ala
NM_000769.4:c.520C>G MANE Select	NP_000760.1:p.Pro174Ala